Canonical Allele Identifier: CA2753880751

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623452C>T , CM000664.2:g.201623452C>T	GRCh38
NC_000002.11:g.202488175C>T , CM000664.1:g.202488175C>T	GRCh37
NC_000002.10:g.202196420C>T	NCBI36
NG_032049.1:g.25078G>A
NG_051007.1:g.731G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*803G>A	ENSP00000480508.2:n.*803G>A
ENST00000686475.1:n.1970G>A
ENST00000409883.7:c.*803G>A MANE Select	ENSP00000386264.2:n.*803G>A
ENST00000409444.6:c.*803G>A	ENSP00000387203.2:n.*803G>A
ENST00000409883.6:c.*803G>A	ENSP00000386264.2:n.*803G>A
ENST00000495329.1:n.1169G>A
NM_001044385.2:c.*803G>A	NP_001037850.1:n.*803G>A
NM_152388.3:c.*803G>A	NP_689601.2:n.*803G>A
NM_001044385.3:c.*803G>A MANE Select	NP_001037850.1:n.*803G>A
NM_152388.4:c.*803G>A	NP_689601.2:n.*803G>A